Urea (Urea Hydrating Topical)

Trade Name : UREA HYDRATING TOPICAL

Acella Pharmaceuticals

AEROSOL, FOAM

Strength 35 g/100g

UREA

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Disclaimer

Trade Marks displayed in compliance with provisions of: Trademark Act, 1999 u/s 30 and 30 (1) of "Fair use"

GNH India is WHO GDP and ISO 9001 2015 Certified Pharmaceutical Wholesaler/ Supplier/ Exporters/ Importer from India of Urea (Urea Hydrating Topical) which is also known as UREA HYDRATING TOPICAL and Manufactured by Acella Pharmaceuticals. It is available in strength of 35 g/100g per ml. Read more

Urea (Urea Hydrating Topical) is supplied for Tenders/ Emergency imports/ Un - licensed, Specials, Orphan drug/ Name patient line/ RLD supplies/ Reference listed drugs/ Comparator Drug/ Bio-Similar/ Innovator samples For Clinical trials. Click to know price. Read less

Packaging and Delivery

Validated Cold Chain Shipment

We deliver your medicines through a validated cold chain shipment process. This process is used as these medicines need to manufactured, transported and stored at very specific temperatures, utilizing thermal and refrigerated packaging methods.

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DESCRIPTIONn n n Urea 35% Hydrating Topical Foam is a keratolytic emollient in a water and lipid based foam containing lactic acid which is a gentle, but potent, tissue softener for skin and nails.n n n Each gram of Urea 35% Hydrating Topical Foam contains Urea 35% as the active ingredient, and the following inactive ingredients: dimethicone, ethylparaben, glycerin, lactic acid,n n n methylparaben, phenoxyethanol, polysorbate 20, povidone, propylene glycol, propylparaben, purified water, stearic acid, trolamine, and in propellants butane and propane.n nn
CHEMICAL STRUCTUREn n n Urea has the following chemical structure:n nn

CLINICAL PHARMACOLOGYn n n Topically applied urea dissolves the intercellular matrix of the skin which results in enhanced shedding of scaly, dry skin and thus a softening of the hyperkeratotic areas of the skin.n n n Urea topically applied to the nail plate has a similar effect on the intercellular matrix of the nail plate.n n n n

PHARMACOKINETICSn n n The mechanism of action of topically applied urea is not yet known.n n n n

INDICATIONS AND USAGEn n n For enzymatic debridement and promotion of normal healing of surface lesions, particularly where healing is retarded by local infection, necrotic tissue, fibrinous or purulent debris,n n n or eschar. Topically applied urea is useful for the treatment of hyperkeratotic conditions such as dermatitis, psoriasis, xerosis, ichthyosis, eczema, keratosis, keratoderma, and dry,n n n rough skin, as well as corns and calluses and damaged, ingrown and devitalized nails.n nn

CONTRAINDICATIONSn n n Known hypersensitivity to any of the listed ingredients.n nn

WARNINGSn n n Urea 35% Hydrating Topical Foam is for external use only. It is not for ophthalmic, oral, anal or intravaginal use. Contact with eyes, lips, and all mucous membranes should ben n n avoided. Urea 35% Hydrating Topical Foam should not be used by persons who have a known hypersensitivity to urea or any of the other listed ingredients.n n n n

PRECAUTIONSn n n Urea 35% Hydrating Topical Foam should be used only as directed by a physician and should not be used to treat any condition other than that for which it is prescribed. If rednessn n n or irritation occurs, discontinue use and consult with a prescribing physician.n n n n

Pregnancy (Category B) u2013 Animal reproduction studies have not been performed with topically applied urea and it is not known whether Urea 35% Hydrating Topical Foam cann n n cause fetal harm when administered to a pregnant woman. Nevertheless, Urea 35% Hydrating Topical Foam should be used by a pregnant woman only if necessary.n n n n

Nursing Mothers u2013 It is not known whether topically applied urea is excreted in human milk. Due to the fact that many drugs are excreted in human milk, caution should ben n n exercised by physicians when administering Urea 35% Hydrating Topical Foam to nursing mothers.n n n n

ADVERSE REACTIONSn n n Transient stinging, burning, itching or irritation is possible.n nn

DOSAGE AND ADMINISTRATIONn n n Unless otherwise directed by a prescribing physician, Urea 35% Hydrating Topical Foam should be applied to affected area twice a day. Urea 35% Hydrating Topical Foam shouldn n n be rubbed into the skin until it is completely absorbed.n n n n

HOW SUPPLIEDn n n Urea 35% Hydrating Topical Foam is supplied in a 150 gram or 5.3 ounce aerosolized canister bearing the NDC Number 42192-115-15.n nn

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NDC 42192-115-15
Urea 35% Hydratingn n nTopical Foamn
Rx Onlyn n nNet Wt. 5.3 oz. (150 g)n
Store at room temperature 59u00b0 - 77u00b0F (15u00b0 - 25u00b0C).n n nSee prescribing information for additional details.n n nIngredients: urea 35%, dimethicone, ethylparaben,n n nglycerin, lactic acid, methylparaben, phenoxyethanol,n n npolysorbate 20, povidone, propylene glycol, propylparaben,n n npurified water, stearic acid, trolamine, and inn n npropellants butane and propane.n
Warning: Contents under pressure. Do not puncture orn n nincinerate. Do not expose to temperatures over 120u00b0Fn n n(48u00b0C) even when empty.n
Keep out of reach of children.
Manufactured for:n n nAcella Pharmaceuticals, LLCn n nAlpharetta, GA 30009n n n1-800-541-4802n n

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Comparator Sourcing for Clinical Trials

GNH India brings over 10 years of experience in Comparator

Name Patient Supply

Today, the exact cause for many rare diseases remains unknown

Validated Cold Chain Shipment

With shifting of pharma industry from synthetic molecules to biologic

Clinical Trials Supply

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GNH Provides Contract Manufacturing services for: Generic Medicines with following

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PRICING POLICY Terms of sales are typically prepaid, unless otherwise

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Urea (Urea Hydrating Topical)

Trade Name : UREA HYDRATING TOPICAL

AEROSOL, FOAM

Delivery Process

Product information is meant for

Disclaimer

Trade Marks displayed in compliance with provisions of: Trademark Act, 1999 u/s 30 and 30 (1) of "Fair use"

Packaging and Delivery

About GNH

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Urea (Urea Hydrating Topical)

Trade Name : UREA HYDRATING TOPICAL

AEROSOL, FOAM

Delivery Process

Product information is meant for

Disclaimer

Trade Marks displayed in compliance with provisions of: Trademark Act, 1999 u/s 30 and 30 (1) of "Fair use"

Packaging and Delivery

About GNH

Similar Products

Desogestrel And Ethinyl Estradiol (Emoquette)

Diphenoxylate Hydrochloride And Atropine Sulfate (Diphenoxylate Hydrochloride And Atropine Sulfate)

Fluoxetine Hydrochloride (Fluoxetine)

Metoprolol Succinate (Metoprolol Succinate)

Losartan Potassium (Losartan Potassium)

Browse Our Services And Processes

Disclaimer

Browse from other international pharmaceuticals

General

US NDC

Canadian DIN

Swiss Drugs

NZ Drugs

FAQ

Can’t find what you’re looking for?

COMPANY

SERVICES

QUICK LINKS

CONTACT US

Can’t find what
you’re looking for?